01 1Cambrex Profarmaco Milano S. r. l.
02 1F. I. S. Fabrica Italiana Sintetici S. p. A.
01 2Chlordiazepoxide
01 1Italy
02 1U.S.A
Registration Number : 218MF10145
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2006-01-31
Latest Date of Registration : 2009-07-21
Registration Number : 222MF10163
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2010-06-02
Latest Date of Registration : 2010-06-02
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PharmaCompass offers a list of Chlordiazepoxide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Chlordiazepoxide manufacturer or Chlordiazepoxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlordiazepoxide manufacturer or Chlordiazepoxide supplier.
A Chloradiazepoxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chloradiazepoxide, including repackagers and relabelers. The FDA regulates Chloradiazepoxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chloradiazepoxide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Chloradiazepoxide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Chloradiazepoxide supplier is an individual or a company that provides Chloradiazepoxide active pharmaceutical ingredient (API) or Chloradiazepoxide finished formulations upon request. The Chloradiazepoxide suppliers may include Chloradiazepoxide API manufacturers, exporters, distributors and traders.
click here to find a list of Chloradiazepoxide suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Chloradiazepoxide Drug Master File in Japan (Chloradiazepoxide JDMF) empowers Chloradiazepoxide API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Chloradiazepoxide JDMF during the approval evaluation for pharmaceutical products. At the time of Chloradiazepoxide JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Chloradiazepoxide suppliers with JDMF on PharmaCompass.
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